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Items: 37

1.

The implication of BDNF Val66Met polymorphism in progression from subjective cognitive decline to mild cognitive impairment and Alzheimer's disease: a 9-year follow-up study.

Bessi V, Mazzeo S, Bagnoli S, Padiglioni S, Carraro M, Piaceri I, Bracco L, Sorbi S, Nacmias B.

Eur Arch Psychiatry Clin Neurosci. 2019 Sep 27. doi: 10.1007/s00406-019-01069-y. [Epub ahead of print]

PMID:
31560105
2.

KIBRA T allele influences memory performance and progression of cognitive decline: a 7-year follow-up study in subjective cognitive decline and mild cognitive impairment.

Mazzeo S, Bessi V, Padiglioni S, Bagnoli S, Bracco L, Sorbi S, Nacmias B.

Neurol Sci. 2019 Aug;40(8):1559-1566. doi: 10.1007/s10072-019-03866-8. Epub 2019 Apr 5.

PMID:
30953258
3.

Crossed aphasia confirmed by fMRI in a case with nonfluent variant of primary progressive aphasia carrying a GRN mutation.

Canu E, Bessi V, Leocadi M, Padiglioni S, Nacmias B, Sorbi S, Filippi M, Agosta F.

J Neurol. 2019 May;266(5):1274-1279. doi: 10.1007/s00415-019-09298-w. Epub 2019 Mar 29.

PMID:
30923936
4.

Acute Symptomatic Sinus Bradycardia in High-Dose Methylprednisolone Therapy in a Woman With Inflammatory Myelitis: A Case Report and Review of the Literature.

Sodero A, Squitieri M, Mazzeo S, Pasca M, Matà S, Pieri F, Bessi V, Sorbi S.

Clin Med Insights Case Rep. 2019 Feb 25;12:1179547619831026. doi: 10.1177/1179547619831026. eCollection 2019.

5.

A Linear Fragment of Unacylated Ghrelin (UAG6-13) Protects Against Myocardial Ischemia/Reperfusion Injury in Mice in a Growth Hormone Secretagogue Receptor-Independent Manner.

Huynh DN, Elimam H, Bessi VL, Ménard L, Burelle Y, Granata R, Carpentier AC, Ong H, Marleau S.

Front Endocrinol (Lausanne). 2019 Jan 11;9:798. doi: 10.3389/fendo.2018.00798. eCollection 2018.

6.

The dual role of cognitive reserve in subjective cognitive decline and mild cognitive impairment: a 7-year follow-up study.

Mazzeo S, Padiglioni S, Bagnoli S, Bracco L, Nacmias B, Sorbi S, Bessi V.

J Neurol. 2019 Feb;266(2):487-497. doi: 10.1007/s00415-018-9164-5. Epub 2019 Jan 2.

PMID:
30604054
7.

Crossed aphasia in nonfluent variant of primary progressive aphasia carrying a GRN mutation.

Bessi V, Piaceri I, Padiglioni S, Bagnoli S, Berti V, Sorbi S, Nacmias B.

J Neurol Sci. 2018 Sep 15;392:34-37. doi: 10.1016/j.jns.2018.06.026. Epub 2018 Jun 30. No abstract available.

PMID:
30097151
8.

From Subjective Cognitive Decline to Alzheimer's Disease: The Predictive Role of Neuropsychological Assessment, Personality Traits, and Cognitive Reserve. A 7-Year Follow-Up Study.

Bessi V, Mazzeo S, Padiglioni S, Piccini C, Nacmias B, Sorbi S, Bracco L.

J Alzheimers Dis. 2018;63(4):1523-1535. doi: 10.3233/JAD-171180.

PMID:
29782316
9.

Association of the New Variant Tyr424Asp at TBK1 Gene with Amyotrophic Lateral Sclerosis and Cognitive Decline.

Piaceri I, Bessi V, Matà S, Polito C, Tedde A, Berti V, Bagnoli S, Braccia A, Del Mastio M, Pignone AM, Pupi A, Sorbi S, Nacmias B.

J Alzheimers Dis. 2018;61(1):41-46. doi: 10.3233/JAD-170694.

PMID:
29103041
10.

Adiponectin has a pivotal role in the cardioprotective effect of CP-3(iv), a selective CD36 azapeptide ligand, after transient coronary artery occlusion in mice.

Huynh DN, Bessi VL, Ménard L, Piquereau J, Proulx C, Febbraio M, Lubell WD, Carpentier AC, Burelle Y, Ong H, Marleau S.

FASEB J. 2018 Feb;32(2):807-818. doi: 10.1096/fj.201700505R. Epub 2018 Jan 4.

PMID:
29018142
11.

Low MT ratio in hippocampus of amnestic MCI patients who will progress to AD.

Mascalchi M, Bessi V, Ginestroni A, Toschi N, Ciulli S, Padiglioni S, Bracco L, Diciotti S.

J Neurol. 2016 May;263(5):1024-1026. doi: 10.1007/s00415-016-8121-4. Epub 2016 Apr 20. No abstract available.

PMID:
27098979
12.

Mutation analysis of patients with neurodegenerative disorders using NeuroX array.

Ghani M, Lang AE, Zinman L, Nacmias B, Sorbi S, Bessi V, Tedde A, Tartaglia MC, Surace EI, Sato C, Moreno D, Xi Z, Hung R, Nalls MA, Singleton A, St George-Hyslop P, Rogaeva E.

Neurobiol Aging. 2015 Jan;36(1):545.e9-14. doi: 10.1016/j.neurobiolaging.2014.07.038. Epub 2014 Aug 1.

13.

Do cholinesterase inhibitors act primarily on attention deficit? A naturalistic study in Alzheimer's disease patients.

Bracco L, Bessi V, Padiglioni S, Marini S, Pepeu G.

J Alzheimers Dis. 2014;40(3):737-42. doi: 10.3233/JAD-131154.

PMID:
24577458
14.

Cooperative role of endogenous leucotrienes and platelet-activating factor in ischaemia-reperfusion-mediated tissue injury.

Bitencourt CS, Bessi VL, Huynh DN, Ménard L, Lefebvre JS, Lévesque T, Hamdan L, Sohouhenou F, Faccioli LH, Borgeat P, Marleau S.

J Cell Mol Med. 2013 Dec;17(12):1554-65. doi: 10.1111/jcmm.12118. Epub 2013 Nov 1.

15.

Protective role of PARK2/Parkin in sepsis-induced cardiac contractile and mitochondrial dysfunction.

Piquereau J, Godin R, Deschênes S, Bessi VL, Mofarrahi M, Hussain SN, Burelle Y.

Autophagy. 2013 Nov 1;9(11):1837-51. doi: 10.4161/auto.26502. Epub 2013 Oct 3.

PMID:
24121678
16.

Regional analysis of the magnetization transfer ratio of the brain in mild Alzheimer disease and amnestic mild cognitive impairment.

Mascalchi M, Ginestroni A, Bessi V, Toschi N, Padiglioni S, Ciulli S, Tessa C, Giannelli M, Bracco L, Diciotti S.

AJNR Am J Neuroradiol. 2013 Nov-Dec;34(11):2098-104. doi: 10.3174/ajnr.A3568. Epub 2013 Jun 6.

17.

TOMM40 polymorphisms in Italian Alzheimer's disease and frontotemporal dementia patients.

Bagnoli S, Piaceri I, Tedde A, Bessi V, Bracco L, Sorbi S, Nacmias B.

Neurol Sci. 2013 Jun;34(6):995-8. doi: 10.1007/s10072-013-1425-6. Epub 2013 Apr 2.

PMID:
23546992
18.

Autosomal dominant frontotemporal lobar degeneration due to the C9ORF72 hexanucleotide repeat expansion: late-onset psychotic clinical presentation.

Galimberti D, Fenoglio C, Serpente M, Villa C, Bonsi R, Arighi A, Fumagalli GG, Del Bo R, Bruni AC, Anfossi M, Clodomiro A, Cupidi C, Nacmias B, Sorbi S, Piaceri I, Bagnoli S, Bessi V, Marcone A, Cerami C, Cappa SF, Filippi M, Agosta F, Magnani G, Comi G, Franceschi M, Rainero I, Giordana MT, Rubino E, Ferrero P, Rogaeva E, Xi Z, Confaloni A, Piscopo P, Bruno G, Talarico G, Cagnin A, Clerici F, Dell'Osso B, Comi GP, Altamura AC, Mariani C, Scarpini E.

Biol Psychiatry. 2013 Sep 1;74(5):384-91. doi: 10.1016/j.biopsych.2013.01.031. Epub 2013 Mar 7.

19.

Identification of mild Alzheimer's disease through automated classification of structural MRI features.

Diciotti S, Ginestroni A, Bessi V, Giannelli M, Tessa C, Bracco L, Mascalchi M, Toschi N.

Conf Proc IEEE Eng Med Biol Soc. 2012;2012:428-31. doi: 10.1109/EMBC.2012.6345959.

PMID:
23365920
20.

A case of atypical early-onset Alzheimer's disease carrying the missense mutation Thr354Ile in exon 10 of the PSEN1 gene.

Marini S, Lucidi G, Tedde A, Bessi V, Nacmias B.

Neurol Sci. 2013 Sep;34(9):1691-2. doi: 10.1007/s10072-012-1260-1. Epub 2012 Dec 2. No abstract available.

PMID:
23212405
21.

A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeats.

van der Zee J, Gijselinck I, Dillen L, Van Langenhove T, Theuns J, Engelborghs S, Philtjens S, Vandenbulcke M, Sleegers K, Sieben A, Bäumer V, Maes G, Corsmit E, Borroni B, Padovani A, Archetti S, Perneczky R, Diehl-Schmid J, de Mendonça A, Miltenberger-Miltenyi G, Pereira S, Pimentel J, Nacmias B, Bagnoli S, Sorbi S, Graff C, Chiang HH, Westerlund M, Sanchez-Valle R, Llado A, Gelpi E, Santana I, Almeida MR, Santiago B, Frisoni G, Zanetti O, Bonvicini C, Synofzik M, Maetzler W, Vom Hagen JM, Schöls L, Heneka MT, Jessen F, Matej R, Parobkova E, Kovacs GG, Ströbel T, Sarafov S, Tournev I, Jordanova A, Danek A, Arzberger T, Fabrizi GM, Testi S, Salmon E, Santens P, Martin JJ, Cras P, Vandenberghe R, De Deyn PP, Cruts M, Van Broeckhoven C, van der Zee J, Gijselinck I, Dillen L, Van Langenhove T, Theuns J, Philtjens S, Sleegers K, Bäumer V, Maes G, Corsmit E, Cruts M, Van Broeckhoven C, van der Zee J, Gijselinck I, Dillen L, Van Langenhove T, Philtjens S, Theuns J, Sleegers K, Bäumer V, Maes G, Cruts M, Van Broeckhoven C, Engelborghs S, De Deyn PP, Cras P, Engelborghs S, De Deyn PP, Vandenbulcke M, Vandenbulcke M, Borroni B, Padovani A, Archetti S, Perneczky R, Diehl-Schmid J, Synofzik M, Maetzler W, Müller Vom Hagen J, Schöls L, Synofzik M, Maetzler W, Müller Vom Hagen J, Schöls L, Heneka MT, Jessen F, Ramirez A, Kurzwelly D, Sachtleben C, Mairer W, de Mendonça A, Miltenberger-Miltenyi G, Pereira S, Firmo C, Pimentel J, Sanchez-Valle R, Llado A, Antonell A, Molinuevo J, Gelpi E, Graff C, Chiang HH, Westerlund M, Graff C, Kinhult Ståhlbom A, Thonberg H, Nennesmo I, Börjesson-Hanson A, Nacmias B, Bagnoli S, Sorbi S, Bessi V, Piaceri I, Santana I, Santiago B, Santana I, Helena Ribeiro M, Rosário Almeida M, Oliveira C, Massano J, Garret C, Pires P, Frisoni G, Zanetti O, Bonvicini C, Sarafov S, Tournev I, Jordanova A, Tournev I, Kovacs GG, Ströbel T, Heneka MT, Jessen F, Ramirez A, Kurzwelly D, Sachtleben C, Mairer W, Jessen F, Matej R, Parobkova E, Danel A, Arzberger T, Maria Fabrizi G, Testi S, Ferrari S, Cavallaro T, Salmon E, Santens P, Cras P; European Early-Onset Dementia Consortium.

Hum Mutat. 2013 Feb;34(2):363-73. doi: 10.1002/humu.22244. Epub 2013 Jan 4.

22.

EP 80317, a selective CD36 ligand, shows cardioprotective effects against post-ischaemic myocardial damage in mice.

Bessi VL, Labbé SM, Huynh DN, Ménard L, Jossart C, Febbraio M, Guérin B, Bentourkia M, Lecomte R, Carpentier AC, Ong H, Marleau S.

Cardiovasc Res. 2012 Oct 1;96(1):99-108. doi: 10.1093/cvr/cvs225. Epub 2012 Jul 10.

PMID:
22787133
23.

Suitability of neuropsychological tests in patients with vascular dementia (VaD).

Bagnoli S, Failli Y, Piaceri I, Rinnoci V, Bessi V, Tedde A, Nacmias B, Sorbi S.

J Neurol Sci. 2012 Nov 15;322(1-2):41-5. doi: 10.1016/j.jns.2012.05.045. Epub 2012 Jun 12. Review.

PMID:
22694976
24.

Implication of serotonin-transporter (5-HTT) gene polymorphism in subjective memory complaints and mild cognitive impairment (MCI).

Marini S, Bagnoli S, Bessi V, Tedde A, Bracco L, Sorbi S, Nacmias B.

Arch Gerontol Geriatr. 2011 Mar-Apr;52(2):e71-4. doi: 10.1016/j.archger.2010.06.006.

PMID:
20599283
25.

Semantic dementia associated with mutation V363I in the tau gene.

Bessi V, Bagnoli S, Nacmias B, Tedde A, Sorbi S, Bracco L.

J Neurol Sci. 2010 Sep 15;296(1-2):112-4. doi: 10.1016/j.jns.2010.06.007. Epub 2010 Jul 3.

PMID:
20598713
26.

Cerebral hemodynamic lateralization during memory tasks as assessed by functional transcranial Doppler (fTCD) sonography: effects of gender and healthy aging.

Bracco L, Bessi V, Alari F, Sforza A, Barilaro A, Marinoni M.

Cortex. 2011 Jun;47(6):750-8. doi: 10.1016/j.cortex.2010.03.007. Epub 2010 Apr 11.

PMID:
20452582
27.

Different implication of NEDD9 genetic variant in early and late-onset Alzheimer's disease.

Tedde A, Bagnoli S, Piaceri I, Lucenteforte E, Bessi V, Bracco L, Mugelli A, Sorbi S, Nacmias B.

Neurosci Lett. 2010 Jun 25;477(3):121-3. doi: 10.1016/j.neulet.2010.04.046. Epub 2010 Apr 27.

PMID:
20430066
28.

Lack of implication for CALHM1 P86L common variation in Italian patients with early and late onset Alzheimer's disease.

Nacmias B, Tedde A, Bagnoli S, Lucenteforte E, Cellini E, Piaceri I, Guarnieri BM, Bessi V, Bracco L, Sorbi S.

J Alzheimers Dis. 2010;20(1):37-41. doi: 10.3233/JAD-2010-1345.

PMID:
20164602
29.

Mild cognitive impairment: loss of linguistic task-induced changes in motor cortex excitability.

Bracco L, Giovannelli F, Bessi V, Borgheresi A, Di Tullio A, Sorbi S, Zaccara G, Cincotta M.

Neurology. 2009 Mar 10;72(10):928-34. doi: 10.1212/01.wnl.0000344153.68679.37.

PMID:
19273828
30.

Early structural changes in individuals at risk of familial Alzheimer's disease: a volumetry and magnetization transfer MR imaging study.

Ginestroni A, Battaglini M, Della Nave R, Moretti M, Tessa C, Giannelli M, Caffarra P, Nacmias B, Bessi V, Sorbi S, Bracco L, De Stefano N, Mascalchi M.

J Neurol. 2009 Jun;256(6):925-32. doi: 10.1007/s00415-009-5044-3. Epub 2009 Mar 1.

PMID:
19252791
31.

KIBRA gene variants are associated with episodic memory performance in subjective memory complaints.

Nacmias B, Bessi V, Bagnoli S, Tedde A, Cellini E, Piccini C, Sorbi S, Bracco L.

Neurosci Lett. 2008 May 9;436(2):145-7. doi: 10.1016/j.neulet.2008.03.008. Epub 2008 Mar 7.

PMID:
18378080
32.

Pattern and progression of cognitive decline in Alzheimer's disease: role of premorbid intelligence and ApoE genotype.

Bracco L, Piccini C, Baccini M, Bessi V, Biancucci F, Nacmias B, Bagnoli S, Sorbi S.

Dement Geriatr Cogn Disord. 2007;24(6):483-91. Epub 2007 Nov 15.

PMID:
18025782
33.

Association of IL10 promoter polymorphism in Italian Alzheimer's disease.

Bagnoli S, Cellini E, Tedde A, Nacmias B, Piacentini S, Bessi V, Bracco L, Sorbi S.

Neurosci Lett. 2007 May 18;418(3):262-5. Epub 2007 Mar 19.

PMID:
17420099
34.

Metabolic correlates of executive dysfunction. Different patterns in mild and very mild Alzheimer's disease.

Bracco L, Bessi V, Piccini C, Mosconi L, Pupi A, Sorbi S.

J Neurol. 2007 Aug;254(8):1052-65. Epub 2007 Mar 25.

PMID:
17385079
35.

Angiotensin converting enzyme insertion/deletion polymorphism in sporadic and familial Alzheimer's disease and longevity.

Nacmias B, Bagnoli S, Tedde A, Cellini E, Bessi V, Guarnieri B, Ortensi L, Piacentini S, Bracco L, Sorbi S.

Arch Gerontol Geriatr. 2007 Sep-Oct;45(2):201-6. Epub 2006 Dec 19.

PMID:
17182125
36.

Hypometabolism exceeds atrophy in presymptomatic early-onset familial Alzheimer's disease.

Mosconi L, Sorbi S, de Leon MJ, Li Y, Nacmias B, Myoung PS, Tsui W, Ginestroni A, Bessi V, Fayyazz M, Caffarra P, Pupi A.

J Nucl Med. 2006 Nov;47(11):1778-86.

37.

Association analysis of the paraoxonase-1 gene with Alzheimer's disease.

Cellini E, Tedde A, Bagnoli S, Nacmias B, Piacentini S, Bessi V, Bracco L, Sorbi S.

Neurosci Lett. 2006 Nov 20;408(3):199-202. Epub 2006 Sep 25.

PMID:
16996683

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